NDC 65293-006 Recothrom
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65293 - The Medicines Company
- 65293-006 - Recothrom
Product Packages
NDC Code 65293-006-41
Package Description: 1 KIT in 1 KIT * 5 mL in 1 VIAL * 5 mL in 1 SYRINGE
Product Details
What is NDC 65293-006?
What are the uses for Recothrom?
Which are Recothrom UNII Codes?
The UNII codes for the active ingredients in this product are:
- THROMBIN ALFA (UNII: SCK81AMR7R)
- THROMBIN ALFA (UNII: SCK81AMR7R) (Active Moiety)
Which are Recothrom Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- MANNITOL (UNII: 3OWL53L36A)
- SUCROSE (UNII: C151H8M554)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- HISTIDINE (UNII: 4QD397987E)
- CALCIUM CHLORIDE (UNII: M4I0D6VV5M)
What is the NDC to RxNorm Crosswalk for Recothrom?
- RxCUI: 1367418 - thrombin alfa 1000 UNT in 1 ML Topical Solution
- RxCUI: 1367418 - thrombin alfa 1000 UNT/ML Topical Solution
- RxCUI: 1367418 - alfa-thrombin 1000 UNT/ML Topical Solution
- RxCUI: 1367418 - thrombin alfa 1000 UNT per 1 ML Topical Solution
- RxCUI: 1367418 - thrombin alfa 20,000 UNT per 20 ML Topical Solution
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".